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Kluver-Bucy Syndrome

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Klüver-Bucy syndrome is a neurobehavioural syndrome associated with bilateral lesions in the anterior temporal horn or amygdala. Heinrich Klüver and Paul Bucy first described the syndrome in 19371 following experimental work where they removed rhesus monkeys' temporal lobes. They found that the monkeys developed:

  1. Visual agnosia - they could see, but were unable to recognise familiar objects or their use.
  2. Oral tendencies - they would examine their surroundings with their mouths instead of their eyes.
  3. Hypermetamorphosis - a desire to explore everything.
  4. Emotional changes - emotion was dulled and facial movements and vocalisations were far less expressive. They lost fear where it would normally occur. Even after being attacked by a snake, they would casually approach it again. This was called "placidity".
  5. Hypersexualism - a dramatic increase in overt sexual behaviour including masturbation, homosexual and heterosexual acts. They may even attempt copulation with inanimate objects.

The syndrome in humans is due to bilateral destruction of the amygdaloid body and inferior temporal cortex, most commonly due to herpes simplex encephalitis.. It shares visual agnosia and loss of normal fear and anger responses in common with the monkey model but one also sees loss of memory with dementia, distractibility and seizures. The hypersexuality tends to be less gross than with the monkeys but may be public and unacceptable.

Epidemiology

It is a very rare disorder and most of the literature relates to animal models rather than human cases:

  • Most literature relating to humans are isolated case reports and few papers report more than a small number of cases.
  • A report of 6 cases has reached the status of further reading for this article with many of the reports originating from India.
  • It is likely to become more common with greater survival of herpes encephalitis due to treatment with antiviral agents.

Risk factors

The most common cause is herpes simplex encephalitis, but it has also been associated with other infections such as tuberculous meningitis or primary cerebral Whipples disease.2

Other causes include:

It has occasionally been described in children.5

Clinical features

Klüver-Bucy syndrome in adults:
Note, we rarely, if ever, see the full syndrome in humans.

  1. Emotional blunting: there is a flat affect and poor response to emotional stimuli (placidity).
  2. Hyperphagia: there is a strong compulsion to place objects in the mouths, probably to gain oral stimulation and to explore the object to counteract the visual agnosia, rather than due to hunger. Nevertheless, there is bulimia and there will be marked weight gain unless diet is restricted. Actions may include socially inappropriate licking or touching.
  3. Visual agnosia: there is an inability to recognise objects or faces visually. This is also called "psychic blindness" ands may account for the oral compulsion.
  4. Increased sexual behaviour: individuals with Klüver-Bucy syndrome lack social sexual restraint with profuse and inappropriate sexual activity.

The syndrome can occur in children and has been reported from India in 7 patients aged 2.5 to 6 years old.5

  • They had all had herpes encephalitis and developed the syndrome on regaining consciousness and activity.
  • Altered emotional behaviour, changes in dietary habits, hyperorality and hypersexuality were present in all, while psychic blindness and hypermetamorphosis occurred in only a few.
  • All showed marked indifference and lack of emotional attachment towards their family.
  • Apathy and easy distractibility were rare.
  • Bulimia and a strong urge to put items other than food into the mouth were common.
  • Hypersexuality presented as frequent holding of genitals, intermittent pelvic thrusting movements and rubbing of genitals to the bed on lying prone. Usually sexually inappropriate behaviour in children is taken as indicative of sexual abuse. There was no suggestion that they had been abused and their ignorance of sex led to a different pattern from adults.
Differential diagnosis

The differential diagnosis usually relates to pinpointing the actual site of the lesion(s) and to cause. Where psychiatric symptoms are predominant, the presence of Klüver-Bucy syndrome suggests a primarily organic cause.6

Management

Non-drug

Patients with Klüver-Bucy syndrome may need careful monitoring to prevent bulimia and consequent obesity but also to prevent uninhibited and inappropriate sexual activity.

Drug

The SSRIs have been shown to be of value7 but carbamazepine may be better.8

Prognosis

Cognitive and behavioural disturbances after herpes encephalitis are often severe but improvement can occur over a long time and residual disabilities vary from major9 to fairly mild.10 The loss of memory is consistent with the hypothesis that medial temporal lobe structures mediate memory consolidation.

Prevention

A paper, also from India, looked at the clinical spectrum, pitfalls in diagnosis and therapeutic implications in herpes simplex encephalitis.11 It concluded that herpes simplex encephalitis is often misdiagnosed, leading to late treatment. Important factors influencing mortality and morbidity are early acyclovir therapy, age, immune status of patient, duration of illness, and consciousness level before initiation of therapy. They advised that acyclovir should be given to all patients as soon as the diagnosis is suspected, whilst awaiting confirmation of diagnosis.


Document references
  1. Kluver H, Bucy PC. Psychic blindness and other symptoms following bilateral temporal lobectomy in rhesus monkeys.; Am J Physiol 1937;119:352-3
  2. Leesch W, Fischer I, Staudinger R, et al; Primary cerebral Whipple disease presenting as Kluver-Bucy syndrome. Arch Neurol. 2009 Jan;66(1):130-1.
  3. Kile SJ, Ellis WG, Olichney JM, et al; Alzheimer abnormalities of the amygdala with Kluver-Bucy syndrome symptoms: an amygdaloid variant of Alzheimer disease. Arch Neurol. 2009 Jan;66(1):125-9. [abstract]
  4. Naito K, Hashimoto T, Ikeda S; Kluver-Bucy syndrome following status epilepticus associated with hepatic encephalopathy. Epilepsy Behav. 2008 Feb;12(2):337-9. Epub 2007 Nov 5. [abstract]
  5. Pradhan S, Singh MN, Pandey N; Kluver Bucy syndrome in young children. Clin Neurol Neurosurg. 1998 Dec;100(4):254-8. [abstract]
  6. Clarke DJ, Brown NS; Kluver-Bucy syndrome and psychiatric illness. Br J Psychiatry. 1990 Sep;157:439-41. [abstract]
  7. Slaughter J, Bobo W, Childers MK; Selective serotonin reuptake inhibitor treatment of post-traumatic Kluver-Bucy syndrome. Brain Inj. 1999 Jan;13(1):59-62. [abstract]
  8. Goscinski I, Kwiatkowski S, Polak J, et al; The Kluver-Bucy syndrome. J Neurosurg Sci. 1997 Sep;41(3):269-72. [abstract]
  9. Pascual-Castroviejo I, Pascual-Pascual SI, Viano J; (Kluver-Bucy syndrome. Seven year follow-up of one patient) Neurologia. 2008 Mar;23(2):114-8. [abstract]
  10. Hart RP, Kwentus JA, Frazier RB, et al; Natural history of Kluver-Bucy syndrome after treated herpes encephalitis. South Med J. 1986 Nov;79(11):1376-8. [abstract]
  11. Jha S, Patel R, Yadav RK, et al; Clinical spectrum, pitfalls in diagnosis and therapeutic implications in herpes simplex encephalitis. J Assoc Physicians India. 2004 Jan;52:24-6. [abstract]

Internet and further reading
  • NINDS; from the American National Institute of Neurological Disorders and Stroke.; KLuver-Bucy Syndrome Information Page
  • Jha S, Patel R; Kluver- Bucy syndrome - An experience with six cases. Neurol India 2004;52:369-371.
Acknowledgements EMIS is grateful to Dr Chloe Borton for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2009.
DocID: 2358
Document Version: 21
DocRef: bgp1247
Last Updated: 27 Jan 2009
Review Date: 27 Jan 2011

The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.

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